Clinical Trials Directory

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UnknownNCT02735629

Antagonism of Opioid-Induced Respiratory Depression by CX1739 With Preservation of Opioid Analgesia

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
18 (actual)
Sponsor
RespireRx · Industry
Sex
Male
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The study is an investigation to assess the capacity of ascending doses of CX1739 to antagonize the respiratory depressive effect of remifentanil. The study will also investigate whether ascending doses of CX1739 reduce the analgesic effect of remifentanil or alter the BIS measure of sedation and will evaluate the safety of CX1739 when used in conjunction with remifentanil.

Conditions

Interventions

TypeNameDescription
DRUGCX1739 - 300 mgAmpakine CX1739 - 300 mg
DRUGCX1739 - 600 mgCX1739 - 600 mg
DRUGCX1739 - 900 mgCX1739 - 900 mg
DRUGPlaceboPlacebo to 300 mg CX1739

Timeline

Start date
2016-03-01
Primary completion
2016-08-01
Completion
2016-09-01
First posted
2016-04-13
Last updated
2016-07-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02735629. Inclusion in this directory is not an endorsement.